Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro

scientific article (publication date: 2013)

Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2013PLoSO...861540T
P356DOI10.1371/JOURNAL.PONE.0061540
P3181OpenCitations bibliographic resource ID3200407
P932PMC publication ID3633995
P698PubMed publication ID23626698
P5875ResearchGate publication ID236461457

P50authorMakoto IkeyaQ51952181
Knut WoltjenQ55135162
Akitsu HottaQ55135226
Satoshi YamashitaQ55277911
Emi ShojiQ59679298
Ken-Ichi IsobeQ88354479
En KimuraQ45857305
P2093author name stringTakuya Yamamoto
Takumi Era
Nobuharu Fujii
Hidetoshi Sakurai
Yasuko Manabe
Atsuko Sehara-Fujisawa
Katsuya Miyake
Akihito Tanaka
Kazunori Hanaoka
Tokiko Nishino
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Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA.Q28131663
Defective membrane repair in dysferlin-deficient muscular dystrophyQ28203095
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyQ28281738
An ECM substratum allows mouse mesodermal cells isolated from the primitive streak to exhibit motility similar to that inside the embryo and reveals a deficiency in the T/T mutant cellsQ28295983
Expression of a single transfected cDNA converts fibroblasts to myoblastsQ29547764
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Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2BQ57990899
The molecular basis of muscular dystrophy in the mdx mouse: a point mutationQ69514522
In vitro synthesis of light and heavy polypeptide chains of myosinQ71585616
Paraxial mesodermal progenitors derived from mouse embryonic stem cells contribute to muscle regeneration via differentiation into muscle satellite cellsQ81198385
piggyBac transposition reprograms fibroblasts to induced pluripotent stem cellsQ29619409
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy geneQ34190227
Plasticity of the differentiated stateQ34379462
Redefining the genetic hierarchies controlling skeletal myogenesis: Pax-3 and Myf-5 act upstream of MyoD.Q34420945
Early expression of the myogenic regulatory gene, myf-5, in precursor cells of skeletal muscle in the mouse embryoQ34500374
MyoD directly up-regulates premyogenic mesoderm factors during induction of skeletal myogenesis in stem cells.Q34509286
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cDNA cloning and mapping of the human creatine kinase M gene to 19q13.Q35198913
Human ES- and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice.Q35947481
MyoD induces myogenic differentiation through cooperation of its NH2- and COOH-terminal regions.Q36320492
Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafishQ36438833
Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B.Q36482213
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Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantationQ41136531
Myogenin, a factor regulating myogenesis, has a domain homologous to MyoD.Q41985465
Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy.Q42819955
Enhanced differentiation of human embryonic stem cells to mesenchymal progenitors by inhibition of TGF-beta/activin/nodal signaling using SB-431542.Q43143526
Myogenic differentiation by human processed lipoaspirate cells.Q46007937
mef2c is activated directly by myogenic basic helix-loop-helix proteins during skeletal muscle development in vivoQ46055034
Mesp2: a novel mouse gene expressed in the presegmented mesoderm and essential for segmentation initiationQ48047260
Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied caseQ48380264
A new model mouse for Duchenne muscular dystrophy produced by 2.4 Mb deletion of dystrophin gene using Cre-loxP recombination systemQ49076566
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectreproducibilityQ1425625
P304page(s)e61540
P577publication date2013-01-01
P1433published inPLOS OneQ564954
P1476titleEfficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro
P478volume8

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